Abstract
Most emerging infectious diseases of humans are transmitted to humans from other animals. The transmission of these “zoonotic” pathogens is affected by the abundance and behavior of their wildlife hosts. However, the effects of infection with zoonotic pathogens on behavior of wildlife hosts, particularly those that might propagate through ecological communities, are not well understood. Borrelia burgdorferi is a bacterium that causes Lyme disease, the most common vector‐borne disease in the USA and Europe. In its North American range, the pathogen is most frequently transmitted among hosts through the bite of infected blacklegged ticks (Ixodes scapularis). Using sham and true vaccines, we experimentally manipulated infection load with this zoonotic pathogen in its most competent wildlife reservoir host, the white‐footed mouse, Peromyscus leucopus, and quantified the effects of infection on mouse foraging behavior, as well as levels of mouse infestation with ticks. Mice treated with the true vaccine had 20% fewer larval blacklegged ticks infesting them compared to mice treated with the sham vaccine, a significant difference. We observed a nonsignificant trend for mice treated with the true vaccine to be more likely to visit experimental foraging trays (20%–30% effect size) and to prey on gypsy moth pupae (5%–20% effect size) compared to mice treated with the sham vaccine. We observed no difference between mice on true‐ versus sham‐vaccinated grids in risk‐averse foraging. Infection with this zoonotic pathogen appears to elicit behavioral changes that might reduce self‐grooming, but other behaviors were affected subtly or not at all. High titers of B. burgdorferi in mice could elicit a self‐reinforcing feedback loop in which reduced grooming increases tick burdens and hence exposure to tick‐borne pathogens.
Highlights
The majority of emerging infectious diseases of humans are transmitted to humans from other vertebrates; that is, they are “zoonotic” (Taylor, Latham, & Woolhouse, 2001; Woolhouse & Gowtage- Sequeria, 2005)
We examined the effects of a widespread zoonotic pathogen, the Lyme disease bacterium Borrelia burgdorferi, on a key reservoir host, the white-footed mouse (Peromyscus leucopus) (Brisson, Dykhuizen, & Ostfeld, 2008; LoGiudice, Ostfeld, Schmidt, & Keesing, 2003)
There was no significant difference in mouse density on grids on which mice were treated with the true vaccine compared to those on which mice were treated with the sham vaccine (Figure 2; mean 63.33 vs. 62.33 [minimum number alive] Kruskal–Wallis p = .37)
Summary
The majority of emerging infectious diseases of humans are transmitted to humans from other vertebrates; that is, they are “zoonotic” (Taylor, Latham, & Woolhouse, 2001; Woolhouse & Gowtage- Sequeria, 2005). We examined the effects of a widespread zoonotic pathogen, the Lyme disease bacterium Borrelia burgdorferi (hereafter Bb), on a key reservoir host, the white-footed mouse (Peromyscus leucopus) (Brisson, Dykhuizen, & Ostfeld, 2008; LoGiudice, Ostfeld, Schmidt, & Keesing, 2003). To determine the effects of Bb on ecological interactions in forests, we experimentally manipulated Bb infection loads in mice using an injectable anti-Bb vaccine patterned after Tsao et al (2004) as well as a control vaccine Using these vaccines, we assessed the effects of Bb infection load on movement and foraging behavior by mice. We measured foraging behavior indirectly by focusing on whether Bb infection load affected risk aversion by mice This is a key behavior affecting interactions between mice and their prey—gypsy moths, ground-nesting songbirds, and tree seeds (Schmidt & Ostfeld, 2008; Schwanz, Previtali, Gomes- Solecki, Brisson, & Ostfeld, 2012). If high Bb infection load reduces the intensity of self-grooming behavior, we expected mice on the anti- Bb-vaccinated plots to have lower tick burdens
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